Soothe XP Preservative Free
NDC 24208-742, light mineral oil and mineral oil, solution/ drops, from Bausch & Lomb Incorporated.
- Product NDC
- 24208-742
- Status
- Listed
- Labeler
- Bausch & Lomb Incorporated
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M018
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/24208-742 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LIGHT MINERAL OIL10 mg/mL
- MINERAL OIL45 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 24208-742-01 | 24208074201 | 30 VIAL, SINGLE-USE in 1 CARTON (24208-742-01) / .3 mL in 1 VIAL, SINGLE-USE |
| 24208-742-99 | 24208074299 | 5 VIAL, SINGLE-USE in 1 POUCH (24208-742-99) / .3 mL in 1 VIAL, SINGLE-USE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 24208-742 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/24208-742 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 24208-742. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.